510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K910438Substantially Equivalent

Dipstick Salmonella

Ampcor, Inc., Bridgeport NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K910438 is the FDA 510(k) clearance record for DIPSTICK SALMONELLA, a class II device, cleared for Ampcor, Inc. on under FDA product code GRM (Antisera, All Groups, Salmonella Spp.). FDA records list 15 510(k) clearances for Ampcor, Inc., from to . As of , FDA records show no recalls naming K910438.

Clearance record

Decision date
Received
(225 days to decision)
Product code
GRM Antisera, All Groups, Salmonella Spp.
Regulation
21 CFR 866.3550
Device class
Class II
Review panel
Microbiology
Applicant
Ampcor, Inc. 510 Heron Dr., Bldg. 306, Bridgeport NJ
Third party review
No

Clearances, product code GRM

Trailing 12 months

FDA records hold no clearances under product code GRM in the trailing twelve months.

FDA records show no clearances under product code GRM in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GRM, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260